Eric Qin has an extensive background in regulatory affairs and quality management within the medical device industry, with notable experience in establishing global regulatory strategies and quality systems. Eric has successfully obtained various certifications and clearances for medical devices from regulatory bodies such as US FDA and EU MDR. Eric has also demonstrated leadership in recall management and conducting risk assessments for high-profile product recalls. With a strong educational background in biomedical engineering and medicine, including a PhD in functional medical imaging, Eric is a highly experienced professional in the field.
August, 2022 - present